Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
-/C | MAF: < 0.01 (-)
Location

Chromosome 19: between 8023388 and 8023389 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

19:g.8023388_8023389insC

Variation displays